InChI
1S/2C7H8O4S2.Zn/c2*8-12(9)6-13(10,11)7-4-2-1-3-5-7;/h2*1-5H,6H2,(H,8,9);/q;;+2/p-2
SMILES string
O=S(O[Zn]OS(CS(=O)(C1=CC=CC=C1)=O)=O)CS(=O)(C2=CC=CC=C2)=O
InChI key
NUNOSEKSQAHHKH-UHFFFAOYSA-L
assay
95% (H-NMR)
form
solid
reaction suitability
reaction type: C-C Bond Formation, reaction type: C-H Activation, reagent type: catalyst
functional group
sulfinic acid, sulfone
storage temp.
2-8°C
Application
New reagent is inspired by nature′s methylating agent, S-adenosyl methionine (SAM). Nitrogen-containing heterocycles can be effectively methylated through a routine two-step route.
C–H Methylation of Heteroarenes Inspired by Radical SAM Methyl Transferase
Profound Methyl Effects in Drug Discovery and a Call for New C H Methylation Reactions
Learn More at the Professor and Product Portal of Professor Phil S. Baran.
C–H Methylation of Heteroarenes Inspired by Radical SAM Methyl Transferase
Profound Methyl Effects in Drug Discovery and a Call for New C H Methylation Reactions
Learn More at the Professor and Product Portal of Professor Phil S. Baran.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
商品
Rapidly diversify (hetero)aromatic scaffolds for chemical industry needs amid resource and time constraints, ensuring efficiency.
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